Seed longevity in terrestrial orchids - Potential for persistent in situ seed banks

Terrestrial orchids typically produce numerous small seeds that contain very small nutrient reserves. The seeds are structurally adapted for wind dispersal but little is known about their fate after dispersal. Some studies of seed viability in situ indicate survival for up to two years in temperate orchid species. Seeds stored in the laboratory may last much longer. We investigated seed viability of seven North American orchid species with seed packets buried in a range of soil and wood substrates within their natural habitats. In Goodyera pubescens most seeds germinated within one year. Four other species continued to germinate sparsely during the observation period, but after almost seven years many seeds were still viable. In one species, Liparis liliifolia, seeds that had been in situ for four years had germination rates as high as 68% when sown in vitro with a compatible fungus. The remaining two species did not germinate during the observation period but the seeds were judged to be intact and tested positively for viability after four years in the ground. These observations are interpreted as different species-specific strategies for in situ germination and their seed bank potential is discussed.     

Intensive management fails to promote recruitment in the last large population of Juniperus communis (L.) in Flanders (Belgium)

In this study, the effectiveness of management measures aimed at promoting recruitment in the last large Flemish juniper population at Heiderbos is evaluated. We resurveyed demographic plots 23 years after their establishment in 1980 and linked the population changes with detailed records of the intensive management during the same period. Between 1980 and 2003 the population size has decreased by 36% and has changed from a relatively immature to a mature population with very few young individuals. Based on a simple model that simulated height growth between 1980 and 2003, the recruitment and mortality rates were estimated to be 5 and 24 ha⁻¹ yr⁻¹, respectively. Intensive management has thus not been able to promote recruitment and the population might go extinct within 40 years if these rates remain unchanged. Furthermore, some measures, notably the working of the soil, have increased mortality of established junipers. The reasons for the limited recruitment are not entirely clear yet, but it may be due to a combination of the limited availability of bare ground for germination and the extremely low viability of juniper seeds. The latter fact may be a common characteristic of many threatened juniper populations in northwestern Europe.     

OPTIMAL FARM MANAGEMENT RESPONSES TO EMERGING SOIL SALINISATION IN A DRYLAND CATCHMENT IN EASTERN AUSTRALIA

Secondary salinisation of soil and water resources is an acute management issue over large parts of Australia. This paper focusses on the situation in the Liverpool Plains, where secondary soil salinity is on the increase due to rising saline groundwater tables. The Liverpool Plains are famous for the vast alluvial floodplains where self-mulching black clays provide the production basis for an extensive dryland cropping industry. The farmers there are asking how best to manage their resources under the present hydrological conditions, and are concerned whether their businesses will remain viable in the future. A multi-period programming model is applied to a model farm situation. The objective function reflects the economic paradigm of farming. The model includes a simulation sub-routine which links land use, rainfall and lateral groundwater flow into a point water balance and estimates the salt-affected area. A feedback relationship applies between soil salinity and land productivity. The results of the model suggest that the prevailing cropping practices that rely on long fallowing for soil moisture retention are sub-optimal. Increased cropping frequency increases farm income and reduces on-farm recharge to groundwater. Diversification into lucerne is favourable for the same reasons. Unless trees have commercial value, tree planting is not a favoured option except on salt-affected land. The farm achieves complete on-farm recharge control. However, assuming that the groundwater table rises at a rate of 10 cm per year independent of on-farm recharge, salinisation continues despite these land management changes. The subsequent land productivity losses render the model farm financially unviable in the medium term. Sustaining the productivity of the Liverpool Plains is an issue of reducing recharge to the groundwater system by changing land-use practices throughout the entire catchment. © 1997 John Wiley & Sons, Ltd.     

珙桐外中果皮对贮藏种子生活力的影响

用四唑染色法与目测法相结合测定珙桐种子的生活力。试验表明,在贮藏了近一年的时间里有外果皮、中果皮的种子生活力迅速地从98.0%降到8.0%,而没有外果皮、中果皮的珙桐种子生活力并没有出现明显的变化,表明珙桐果实外果皮、中果皮在种子贮藏期间对珙桐种子的生活力影响非常大。     

不同培养基组分对5个蜡梅品系花粉萌发和花粉管生长的影响

以河南省许昌市3个类型5个品系的蜡梅花粉为试验材料,研究了不同培养基组分对蜡梅花粉萌发和花粉管生长的影响,以筛选出适宜不同类型蜡梅花粉萌发的最佳培养基,为生产实践中科学授粉和杂交育种提供理论依据.结果表明:聚乙二醇是蜡梅花粉萌发和花粉管生长的关键因素,当培养基中没有聚乙二醇时,花粉不能萌发;蔗糖不是蜡梅花粉离体萌发的必...     

Effect of HC-1119 on biological behaviors of triple-negative breast cancer BT549 cells

AIM: To explore the effect of new artificially synthesized androgen receptor (AR) antagonist HC-1119 on the biological function of triple-negative breast cancer (TNBC) BT549 cells and the molecular mechanism. METHODS: The AR expression was assessed in different human breast cancer cell lines MDA-MB-231, T47D, MCF-7, SKBR3 and BT549 by Western blot. The TNBC BT549 cells with AR positive expression were treated with HC-1119. The cell viability was measured by CCK-8 assay. The apoptosis rate and cell cycle distribution were analyzed by flow cytometry. The migration and invasion abilities were detected by Transwell assay in vitro. The protein expression of E-cadherin, vimentin and P21 was determined by Western blot. RESULTS: AR was positively expressed in BT549 cells. HC-1119 inhibited the cell viability in a time-and dose-dependent manner (P<0.05), increased the percentage of apoptotic cells and the percentage of S-phase cells significantly, repressed the migration and invasion abilities (P<0.05), and decreased P21 expression at protein level (P<0.01). No influence on the expression of E-cadherin and vimentin in the BT549 cells was observed. CONCLUSION: AR antagonist HC-1119 decreases the viability, migration ability and invasion ability, enhances the apoptosis, and arrests the cell cycle distribution of TNBC BT549 cells. HC-1119 represses the viability of BT549 cells by down-regulating P21 expression, while the process of epithelial-mesenchymal transition is not involved in the inhibition of cell migration.     

Effect of DEC1 gene silencing on viability,invasion and migration of human breast cancer MDA-MB-231 cells under hypoxia

AIM: To investigate the effect of differentiated embryonic chondrocyte gene 1 (DEC1) expression silencing on viability, invasion and migration of human breast cancer MDA-MB-231 cells and its possible mechanism under hypoxia. METHODS: The expression of DEC1 was detected by RT-qPCR and Western blot in breast cancer MDA-MB-231 cells under normoxia and hypoxia. MDA-MB-231 cells were transfected with the siRNA targeting DEC1 and the protein levels of DEC1, Smad3 and phosphorylated Smad3 (p-Smad3) were examined under hypoxia. Subsequently, the changes in the viability, invasion and migration abilities of MDA-MB-231 cells were analyzed by CCK-8 assay, Transwell experiment and Scratch test, respectively. RESULTS: The expression of DEC1 in MDA-MB-231 cells under hypoxia was higher than that in the MDA-MB-231 cells under normoxia condition at both mRNA and protein levels (P<0.05). The viability, invasion and migration abilities of MDA-MB-231 cells in siRNA-DEC1 group were decreased significantly as compared with control group (P<0.01). Besides, the protein level of p-Smad3 in the MDA-MB-231 cells in siRNA-DEC1 group was lower than that in negative control group under hypoxia condition (P<0.05). CONCLUSION: Down-regulated DEC1 expression significantly decreases the viability, invasion and migration abilities of breast cancer MDA-MB-231 cells by blocking the TGF-β/Smad3 signaling pathway under hypoxia condition.     

MicroRNA-330 inhibits growth and migration of gastric cancer cells by directly targeting EGR-2

AIM:To explore the function and significance of microRNA-330 (miR-330) in the development of gastric cancer. METHODS:Forty-eight cases of gastric cancer tissues and paired adjacent tissues were collected in Department of Oncology, Affiliated Hospital of Gansu University of Chinese Medicine, and the expression levels of miR-330 were detected by RT-qPCR. The expression levels of miR-330 in the gastric cancer cells and human gastric epithelial GES-1 cells were evaluated by RT-qPCR. The viability, colony formation and migration of gastric cancer cells after transfected with miR-330 inhibitor or miR-330 mimic were analyzed by CCK-8 assay, colony formation assay and Transwell assay, respectively. Furthermore, miR-330 target gene was predicted by miRanda target gene prediction database. RESULTS:miR-330 expression was down-regulated both in gastric cancer tissues and gastric cancer cells (P<0.05). The expression levels of miR-330 were negatively associated with the tumor size, lymph metastasis, pathological grade stage and T stage (P<0.05). The viability, colony formation and migration of gastric cancer cells were significantly increased after transfected with miR-330 inhibitor (P<0.05). However, the viability, colony formation and migration of gastric cancer cells were significantly decreased after transfected with miR-330 mimic (P<0.05). Furthermore, EGR-2 was the direct target gene of miR-330. CONCLUSION:miR-330 suppresses gastric cancer cell growth and migration, and the mechanism may be related to its direct target gene EGR-2, suggesting that miR-330 may be used as a potential new target for diagnosis and targeted therapy for gastric cancer.     

VEGF promotes biliary epithelial cell viability and cystic dilation in rats with polycystic kidney

AIM:To explore the promoting effect of vascular endothelial growth factor (VEGF) on the viability of biliary epithelial cells and biliary cystic dilation in rats with polycystic kidney (PCK). METHODS:Immunohistoche-mical staining was used to detect the expression of VEGF (n=6) and CD31 (n=10) in the liver tissue of normal and PCK rats. RT-qPCR and ELISA were used to evaluate the expression levels of VEGF in rat biliary epithelial cells and culture supernatant. WST-1 assay was applied to measure the effect of VEGF on the viability of rat biliary epithelial cells, and the influence of cholangiocyte culture supernatant on the viability of rat vascular endothelial cells. The cell migration assay was employed to observe the effect of cholangiocyte culture supernatant on endothelial cell migration. Tube formation assay was used to assess the impact of cholangiocyte culture supernatant on the angiogenic ability of endothelial cells. RESULTS:The result of immunohistochemical staining manifested that VEGF was highly expressed in the cholangiocytes of the PCK rats (P<0.01). More newly formed blood vessels were observed in the hepatic portal area of PCK rats than that in normal rats (P<0.01). The results of RT-qPCR and ELISA suggested that the mRNA and protein expression levels of VEGF in the cholangiocytes of PCK rats were significantly higher than those in normal rats (P<0.01). VEGF enhanced the viability of cholangiocytes in PCK rats (P<0.01). The culture supernatant of cholangiocytes in PCK rats increased the endothelial cell viability (P<0.01). VEGF siRNA and VEGF receptor inhibitor reduced the viability of cholangiocytes (P<0.01). The results of cell migration assay and tube formation assay indicated that the abilities of endothelial cell migration and tube formation were improved by the culture supernatant of cholangiocytes in PCK rats (P<0.01). CONCLUSION:The bile duct cystic dilation of PCK rats was related to the excessive secretion of VEGF in bile duct epithelial cells.